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(RS)-rapamycin

group of stereoisomers with the chemical formula C₅₁H₇₉NO₁₃
ChemicalSubstance group_of_stereoisomers Q27163227
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(RS)-rapamycin

Summary

(RS)-rapamycin is a group of stereoisomers[1].

Key Facts

  • (RS)-rapamycin's instance of is recorded as group of stereoisomers[2].
  • (RS)-rapamycin's canonical SMILES is recorded as CC1CCC2CC(C(=CC=CC=CC(CC(C(=O)C(C(C(=CC(C(=O)CC(OC(=O)C3CCCCN3C(=O)C(=O)C1(O2)O)C(C)CC4CCC(C(C4)OC)O)C)C)O)OC)C)C)C)OC[3].
  • (RS)-rapamycin's InChI is recorded as InChI=1S/C51H79NO13/c1-30-16-12-11-13-17-31(2)42(61-8)28-38-21-19-36(7)51(60,65-38)48(57)49(58)52-23-15-14-18-39(52)50(59)64-43(33(4)26-37-20-22-40(53)44(27-37)62-9)29-41(54)32(3)25-35(6)46(56)47(63-10)45(55)34(5)24-30/h11-13,16-17,25,30,32-34,36-40,42-44,46-47,53,56,60H,14-15,18-24,26-29H2,1-10H3[4].
  • (RS)-rapamycin's InChIKey is recorded as QFJCIRLUMZQUOT-UHFFFAOYSA-N[5].
  • (RS)-rapamycin's chemical formula is recorded as C₅₁H₇₉NO₁₃[6].
  • (RS)-rapamycin's subclass of is recorded as macrolides[7].
  • (RS)-rapamycin's subclass of is recorded as triol[8].
  • (RS)-rapamycin's subclass of is recorded as piperidine[9].
  • (RS)-rapamycin's subclass of is recorded as tetrahydropyran[10].
  • (RS)-rapamycin's subclass of is recorded as N,N-disubstituted primary carboxamide[11].
  • (RS)-rapamycin's subclass of is recorded as methyl ether[12].
  • (RS)-rapamycin's ChEMBL ID is recorded as CHEMBL3560003[13].
  • (RS)-rapamycin's PubChem CID is recorded as 5040[14].
  • (RS)-rapamycin's ChEBI ID is recorded as 91355[15].
  • (RS)-rapamycin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+913.555'}[16].
  • (RS)-rapamycin's SureChEMBL ID is recorded as 386130[17].
  • (RS)-rapamycin's UniChem compound ID is recorded as 53943732[18].
  • (RS)-rapamycin's Probes And Drugs ID is recorded as PD003274[19].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . ChEBI. Retrieved . wikidata.org.
  15. [16] ↑ . PubChem. Retrieved . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . UniChem. wikidata.org.
  18. [19] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). (RS)-rapamycin. Retrieved May 3, 2026, from https://4ort.xyz/entity/-rs-rapamycin
MLA “(RS)-rapamycin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-rs-rapamycin.
BibTeX @misc{4ortxyz_-rs-rapamycin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(RS)-rapamycin}}, year = {2026}, url = {https://4ort.xyz/entity/-rs-rapamycin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (RS)-rapamycin — https://4ort.xyz/entity/-rs-rapamycin (retrieved 2026-05-03)

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